Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children

Am J Med Genet. 1995 Mar 13;56(1):106-11. doi: 10.1002/ajmg.1320560124.


We report on an unselected group of 24 children with small supernumerary marker chromosomes, found in a large sample of 34,910 consecutive newborns karyotyped at birth. Sixteen of these were available for reexamination. With the use of in situ hybridization with alpha-satellite centromere probes and satellite III, ribosomal and beta-satellite DNA probes, we have characterized these markers. In 14 of the 16 cases we have been able to determine the chromosomal origin of the marker. Twelve of the markers are derived from the acrocentric chromosomes. Of these 12 markers, 4 are derived from chromosome 14, 4 from chromosome 22, 3 from chromosome 15 and one is from either chromosome 13 or 21. Ten of these markers were initially ascertained with the satellite III DNA probe, taking advantage of the fact that satellite III DNA is found in the centromeric region of the following chromosomes: 1, 5, 9, 13, 14, 15, 16, 20, 21, 22, and Y. Two markers were derived from chromosomes 4 and 8. The origin of the last 2 markers could not be determined with the techniques employed. Only one of these children is psychometrically retarded and has a peculiar appearance. Unfortunately we were not able to determine the origin of the marker in her case. All other children developed normally.

Publication types

  • Review

MeSH terms

  • Centromere / genetics
  • Chromosome Aberrations / genetics*
  • Chromosome Banding
  • Chromosomes, Human, 13-15 / genetics
  • Chromosomes, Human, 21-22 and Y / genetics
  • Chromosomes, Human, Pair 4 / genetics
  • Chromosomes, Human, Pair 8 / genetics
  • DNA / blood
  • Female
  • Genetic Markers
  • Humans
  • Infant, Newborn
  • Male
  • Prospective Studies


  • Genetic Markers
  • DNA